Phenylpropiolic Acid → HCID 20613746, compound
Reaction equation
Cl.Cl.[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@@H:5]([NH2:11])[CH2:4]2.[C:12]1([C:18]#[C:19][C:20](O)=[O:21])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@@H:5]([NH:11][C:20](=[O:21])[C:19]#[C:18][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:4]2Participants
3
Procedure
Prepared as a free base by a method analogous to that described in Example 1 from (R)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride and 3-phenylpropynoic acid; MS (ES+) 255 (MH+).
Workup
- customPrepared as a free base by a method analogous to
Sources & evidence
- ORD record
- ord-672f90d5c07e4cbea16d7b5121396c76
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683090B1
Reaction notes
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